- Merck & Co. (Rahway, NJ)
- …and ensures continuity of site relationships through all phases of the trial .Performs clinical study site management/monitoring activities in compliance with ... oversight of the CRA manager or CRD, the person ensures compliance of study conduct with ICH/GCP and country regulations, our company's policies and procedures,… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …areas centered around rare diseases and immune disorders. Summary The Associate Director, Quantitative Systems Pharmacology (QSP) will work within the Quantitative ... include target prioritization, therapeutic modality selection, biomarker characterization and clinical trial design. In addition, he/she will develop a QSP strategy… more
- Boehringer Ingelheim (Ridgefield, CT)
- …+ Accountable for optimal planning, interpretation and data presentation of clinical studies from FIM throughout pivotal studies , ensuring integration of ... and other contributors), Clinical Development Plans or similar documents, Core Clinical Trial Protocols, including the CTP strategy and core CTP elements within a… more
- Guidehouse (Bethesda, MD)
- …completeness of documents. + Assist researchers collect, organize, and maintain all study documentation to include investigator qualifications, trial logs, and ... regulatory related documentation description. + Collect, organize, and maintain all study documentation to include investigator qualifications, trial logs, and… more
- IQVIA (Durham, NC)
- **PURPOSE** IQVIA Design Analytics delivers clinical trial design optimization services that integrates drug development and clinical trial expertise with real ... world data, transformative technologies, methods, and work models. The Associate Design Analytics Director primarily supports client consulting engagements,… more
- Merck (Columbus, OH)
- …and ensures continuity of site relationships through all phases of the trial . + Performs clinical study site management/monitoring activities in compliance ... oversight of the CRA manager or CRD, the person ensures compliance of study conduct with ICH/GCP and country regulations, our company's policies and procedures,… more
- Pennsylvania State University (University Park, PA)
- …. JOB DESCRIPTION AND POSITION REQUIREMENTS: Part-Time Junior Policy Associate : Paid Internship to Implement a BIPOC Policy Scholars Program ... connecting legislative officials with those who specialize in data and scientific study relevant to policymakers' current policy agendas. This also provides a… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …areas centered around rare diseases and immune disorders. **Summary** The Associate Director, Quantitative Systems Pharmacology (QSP) will work within the ... include target prioritization, therapeutic modality selection, biomarker characterization and clinical trial design. In addition, he/she will develop a QSP strategy… more
- UCLA Health (Los Angeles, CA)
- …mobile scalp and intracranial EEG, electro-, and psychophysiological recordings on study participants; perform task presentation using virtual and augmented ... for research projects in a neuromodulation and neuroimaging laboratory; perform pre- study interviews of participants and families, consent of participants, and… more
- Bristol Myers Squibb (Princeton, NJ)
- …selection, chemical/biotherapeutic optimization, biomarker characterization, combination assessment, clinical trial design, and trial interpretation. Our ... project teams to design, execute and interpret preclinical and clinical studies + Independently collaborate with stakeholders to identify and interpret experiments… more
- University of Utah (Salt Lake City, UT)
- …sponsors to communicate and resolve issues Assumes considerable leadership responsibilities of studies throughout the network Provides feedback on study site ... offers opportunities to work with high functioning, cutting-edge teams that study , understand and improve multi-site research. Bring your background in strong… more
- University of Colorado (Aurora, CO)
- …all the affiliated sites in the I-SCREEN Hub. + Direct activities related to study procedure and set up in accordance with NCI/CTEP requirements including but not ... with other I-SCREEN staff and investigators to facilitate I-SCREEN study start up and recruitment activities. + Participate in...participate in the annual CSRN in-person meetings and other virtual meetings as required. + Utilize resources in the… more
- US Army Corps of Engineers (San Francisco, CA)
- …as a GS-04, students must have completed two full academic years of post-high school study or have an associate 's degree. To qualify for a Pathways Internship as ... programs completed) are not considered an academic course of study . Internship for current students in good standing at...provide proof of US Citizenship, as applicable. Two year trial /probationary period may be required. Direct Deposit of Pay… more
- Boehringer Ingelheim (Ridgefield, CT)
- …In alignment with Clinical Operations, interacting with current and potential BI study investigators to support clinical trial activities. + Facilitating ... logistical communications between BIPI and HCPs regarding Investigator Initiated Studies (IIS), External Collaborative Research, company study contracts, etc.,… more
